NARA Discovery
Article Details
← Back to Search Results
Journal Article

Environmental formation of methylmercury is controlled by synergy of inorganic mercury bioavailability and microbial mercury‐methylation capacity

Benjamin D. Peterson; David P. Krabbenhoft; Katherine D. McMahon; Jacob M. Ogorek; Michael T. Tate; William H. Orem; Brett A. Poulin
Environmental Microbiology · Vol. 25, Issue 8 · pp. 1409-1423 · 2023

Abstract

Methylmercury (MeHg) production is controlled by the bioavailability of inorganic divalent mercury (Hg(II) i ) and Hg‐methylation capacity of the microbial community (conferred by the hgcAB gene cluster). However, the relative importance of these factors and their interaction in the environment remain poorly understood. Here, metagenomic sequencing and a full‐factorial MeHg formation experiment were conducted across a wetland sulfate gradient with different microbial communities and pore water chemistries. From this experiment, the relative importance of each factor on MeHg formation was isolated. Hg(II) i bioavailability correlated with the dissolved organic matter composition, while the microbial Hg‐methylation capacity correlated with the abundance of hgcA genes. MeHg formation responded synergistically to both factors. Notably, hgcA sequences were from diverse taxonomic groups, none of which contained genes for dissimilatory sulfate reduction. This work expands our understanding of the geochemical and microbial constraints on MeHg formation in situ and provides an experimental framework for further mechanistic studies.

Bibliographic Information

JournalEnvironmental Microbiology
PublisherWiley
Publication Date2023-08-01
Publication Year2023
Volume25
Issue8
Pages1409-1423
Document TypeJournal Article
Print ISSN1462-2912
eISSN1462-2920
DOI10.1111/1462-2920.16364
SubjectMicrobial Ecology

Access Information

NARA Access Coverage1999-01-01~Current
Journal Homepagehttps://onlinelibrary.wiley.com/loi/14622920
Publisher PageOpen Publisher Page
Full-text access depends on NARA's subscribed coverage and institutional access.